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霍奇金病患者亲属中总T淋巴细胞的定量及功能异常

Quantitative and functional abnormalities of total T lymphocytes in relatives of patients with Hodgkin's disease.

作者信息

del Giacco G S, Cengiarotti L, Mantovani G, Murgia M, Broccia G, Corda G, di Tucci A

出版信息

Eur J Cancer Clin Oncol. 1985 Jul;21(7):793-801. doi: 10.1016/0277-5379(85)90217-2.

Abstract

Seven patients, long-term survivors of Hodgkin's disease, and 24 of their relatives (parents, siblings and children), together with normal controls were studied for percentages, absolute counts and mitogen-proliferative responses by means of monoclonal antibodies, E rosette technique and in vitro cultures with PHA, ConA and PWM. The aim of the study was to ascertain whether the impaired cell-mediated immunity of Hodgkin's patients was also present in relatives in order to elucidate the still debated etiology of the defect and of the disease (congenital? environmental? infectious?). The results show that both Hodgkin's patients and their relatives have a significant decrease of total T cells (as T3+, T11+ and E rosette-forming cells) in peripheral blood and a significant impairment of polyclonal responses to all the mitogens employed. The Leu-7+ cells (i.e. a consistent amount of natural killer cells) are significantly increased only in the Hodgkin's patients but not in their relatives. The T cell subpopulations (T4 and T8), B cells and monocytes do not show any difference between the patients, their relatives and normal controls. Our results seem to support, at least in part, the presence of a common defect of T cell lineage both in patients and in their relatives, but its etiology still remains uncertain (genetic? environmental?).

摘要

对7例霍奇金病长期存活者及其24名亲属(父母、兄弟姐妹和子女)以及正常对照者,采用单克隆抗体、E花环技术以及用PHA、ConA和PWM进行体外培养的方法,研究其细胞百分比、绝对计数和丝裂原增殖反应。本研究的目的是确定霍奇金病患者受损的细胞介导免疫在其亲属中是否也存在,以便阐明该缺陷及疾病(先天性?环境因素?感染性?)仍存在争议的病因。结果显示,霍奇金病患者及其亲属外周血中的总T细胞(如T3 +、T11 +和E花环形成细胞)均显著减少,对所有所用丝裂原的多克隆反应均显著受损。Leu - 7 +细胞(即相当数量的自然杀伤细胞)仅在霍奇金病患者中显著增加,而在其亲属中未增加。患者、其亲属和正常对照者之间的T细胞亚群(T4和T8)、B细胞和单核细胞没有任何差异。我们的结果似乎至少部分支持患者及其亲属中存在T细胞系的共同缺陷,但其病因仍不确定(遗传因素?环境因素?)

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